Prune belly syndrome associated with bilateral multicystic dysplastic kidneys and urethral obstruction: A case report
Prune belly syndrome is a rare congenital disorder defined by a characteristic clinical triad: Abdominal muscle deficiency, severe urinary tract abnormalities, and bilateral cryptorchidism. We describe a preterm neonate of Prune Belly syndrome who had abdominal muscle deficiency, multicystic dysplas...
Main Authors: | Arzu Akdag, Sule Arici, Betul Orhaner, Anil Dogan |
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Format: | Article |
Language: | English |
Published: |
Ped Urol Case Rep
2015-06-01
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Series: | Pediatric Urology Case Reports |
Subjects: | |
Online Access: | http://pediatricurologycasereports.com/ojs/index.php/pucr/article/view/79/53 |
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